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Published on: November 5, 2019
Sickle cell disease and the kidney.
Abdou Niang1, Boucar Diouf, Fatou S Ndiaye Sene
1Clinique Médicale 1, Centre hospitalier Universitaire A. Le Dantec, Dakar, Senegal.
Sickle cell disease (SCD) in West Africa presents diverse renal changes, including chronic glomerulonephritis and renal failure. Early diagnosis and multidisciplinary care are crucial for managing these kidney complications.
Area of Science:
- Nephrology
- Hematology
- Public Health
Background:
- Sickle cell disease (SCD) is prevalent in West Africa, yet its renal manifestations and outcomes remain under-characterized.
- Understanding the spectrum of kidney disease in SCD patients is vital for improving patient management.
Purpose of the Study:
- To retrospectively investigate the types and prevalence of renal abnormalities in West African patients with sickle cell trait (AS) and sickle cell disease (SS).
- To characterize the renal outcomes and histopathological findings in this population.
Main Methods:
- Retrospective analysis of 22 renal patients with sickle cell hemoglobin (19 AS, 3 SS) between 1996 and 2002.
- Review of clinical data, diagnoses of nephropathies, and renal biopsy findings in a subset of patients.
Main Results:
- Common nephropathies included chronic glomerulonephritis (36.3%), advanced chronic renal failure (31.8%), and chronic tubulointerstitial nephropathy (18.1%).
- Renal biopsies revealed conditions such as membranoproliferative glomerulonephritis, focal and segmental glomerulosclerosis, and membranous glomerulonephritis.
Conclusions:
- Sickle cell disease is associated with a variety of renal abnormalities in the West African population.
- Optimal management necessitates early diagnosis and a multidisciplinary approach for effective follow-up and treatment.
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